Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g55480 | A09 | 55608430 | G | A | missense_variant | MODERATE | c.1069G>A|p.Glu357Lys |
S107 |
2 | BAA09g55480 | A09 | 55608970 | C | T | missense_variant | MODERATE | c.1609C>T|p.Pro537Ser |
S192 |
3 | BAA09g55480 | A09 | 55609150 | C | T | missense_variant | MODERATE | c.1789C>T|p.Pro597Ser |
S35 |
4 | BAA09g55480 | A09 | 55609376 | C | T | missense_variant | MODERATE | c.2015C>T|p.Pro672Leu |
S152 |
5 | BAA09g55480 | A09 | 55609748 | C | T | synonymous_variant | LOW | c.2304C>T|p.Phe768Phe |
S242 |
6 | BAA09g55480 | A09 | 55611045 | C | T | missense_variant | MODERATE | c.2905C>T|p.Leu969Phe |
S35 |
7 | BAA09g55480 | A09 | 55611407 | C | T | splice_region_variant&intron_variant | LOW | c.3102+6C>T| |
S133 |
8 | BAA09g55480 | A09 | 55611542 | C | T | missense_variant | MODERATE | c.3155C>T|p.Ser1052Phe |
S99 |
9 | BAA09g55480 | A09 | 55611695 | C | T | missense_variant | MODERATE | c.3214C>T|p.Pro1072Ser |
S229 |
10 | BAA09g55480 | A09 | 55614531 | G | A | downstream_gene_variant | MODIFIER | c.*2570G>A| |
S236 |
11 | BAA09g55480 | A09 | 55614586 | C | T | downstream_gene_variant | MODIFIER | c.*2625C>T| |
S61 |
12 | BAA09g55480 | A09 | 55614842 | C | T | downstream_gene_variant | MODIFIER | c.*2881C>T| |
S192 |